ClinVar Miner

List of variants in gene ATP6V0A2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP
NC_000012.12:g.123712055T>A rs767739299
NM_012463.3(ATP6V0A2):c.-227A>G rs561163813
NM_012463.4(ATP6V0A2):c.1039-13G>T rs375793162
NM_012463.4(ATP6V0A2):c.1128C>T (p.Thr376=) rs138172178
NM_012463.4(ATP6V0A2):c.117+14G>A rs144930749
NM_012463.4(ATP6V0A2):c.117+17_117+20delinsTCT rs1555295264
NM_012463.4(ATP6V0A2):c.118-73G>A rs114594614
NM_012463.4(ATP6V0A2):c.1189+12G>T rs377235629
NM_012463.4(ATP6V0A2):c.1194C>T (p.Leu398=) rs775345155
NM_012463.4(ATP6V0A2):c.1215G>A (p.Pro405=) rs1171365721
NM_012463.4(ATP6V0A2):c.1258G>T (p.Val420Leu) rs138716143
NM_012463.4(ATP6V0A2):c.1327-16G>A rs149092701
NM_012463.4(ATP6V0A2):c.1452C>T (p.Asn484=) rs567406924
NM_012463.4(ATP6V0A2):c.1485C>T (p.Pro495=) rs759980365
NM_012463.4(ATP6V0A2):c.1590C>T (p.Pro530=) rs80355657
NM_012463.4(ATP6V0A2):c.1698A>G (p.Gly566=) rs2271659
NM_012463.4(ATP6V0A2):c.1724+20T>A rs778282853
NM_012463.4(ATP6V0A2):c.1935+75T>C rs138200834
NM_012463.4(ATP6V0A2):c.1936-147C>T rs80175450
NM_012463.4(ATP6V0A2):c.1936-7C>T rs370135665
NM_012463.4(ATP6V0A2):c.196+15T>G rs1404046246
NM_012463.4(ATP6V0A2):c.2014T>C (p.Leu672=) rs367950442
NM_012463.4(ATP6V0A2):c.2056-14C>G rs375232199
NM_012463.4(ATP6V0A2):c.2148T>C (p.Asp716=) rs962207534
NM_012463.4(ATP6V0A2):c.2229T>C (p.Cys743=) rs150508296
NM_012463.4(ATP6V0A2):c.2238C>T (p.Cys746=) rs138886791
NM_012463.4(ATP6V0A2):c.2294-4G>A rs551697992
NM_012463.4(ATP6V0A2):c.2308C>T (p.Leu770=) rs149439834
NM_012463.4(ATP6V0A2):c.2340C>T (p.Arg780=) rs201694504
NM_012463.4(ATP6V0A2):c.2367A>G (p.Leu789=) rs142041624
NM_012463.4(ATP6V0A2):c.2469A>G (p.Val823=) rs775830030
NM_012463.4(ATP6V0A2):c.264G>A (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.264G>T (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.295-17C>A rs1555296412
NM_012463.4(ATP6V0A2):c.432+12C>T rs535259667
NM_012463.4(ATP6V0A2):c.447T>C (p.Tyr149=) rs140835376
NM_012463.4(ATP6V0A2):c.521+14C>G rs747194853
NM_012463.4(ATP6V0A2):c.521+14C>T rs747194853
NM_012463.4(ATP6V0A2):c.521+17G>A rs192339944
NM_012463.4(ATP6V0A2):c.522-13del rs140638516
NM_012463.4(ATP6V0A2):c.649-36G>A rs143993135
NM_012463.4(ATP6V0A2):c.732-3C>T rs1371899202
NM_012463.4(ATP6V0A2):c.768C>T (p.Ala256=) rs373419502
NM_012463.4(ATP6V0A2):c.795G>A (p.Gly265=) rs754399086
NM_012463.4(ATP6V0A2):c.840C>A (p.Thr280=) rs139680786
NM_012463.4(ATP6V0A2):c.853A>C (p.Arg285=) rs776563027
NM_012463.4(ATP6V0A2):c.993C>T (p.Pro331=) rs367873118

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.